Canonical Allele Identifier: CA2690817827

Gene: HSD17B3 HSD17B3-AS1

Linked Data

• gnomAD v4: 9-96251196-A-AAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96251201_96251203dup , CM000671.2:g.96251201_96251203dup	GRCh38
NC_000009.11:g.99013483_99013485dup , CM000671.1:g.99013483_99013485dup	GRCh37
NC_000009.10:g.98053304_98053306dup	NCBI36
NG_008157.1:g.55954_55956dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.453+219_453+221dup (HSD17B3)	ENSP00000364411.2:n.453+219_453+221dup
ENST00000375263.8:c.453+219_453+221dup (HSD17B3) MANE Select	ENSP00000364412.3:n.453+219_453+221dup
ENST00000463517.2:n.1325_1327dup
ENST00000464104.6:n.986_988dup
ENST00000467499.6:c.*152+219_*152+221dup (HSD17B3)	ENSP00000498077.1:n.*152+219_*152+221dup
ENST00000643789.1:c.2745+219_2745+221dup
ENST00000648146.1:c.453+219_453+221dup (HSD17B3)	ENSP00000497238.1:n.453+219_453+221dup
ENST00000648332.1:c.202-5773_202-5771dup (HSD17B3)	ENSP00000497562.1:n.202-5773_202-5771dup
ENST00000648799.1:c.345+219_345+221dup (HSD17B3)	ENSP00000498039.1:n.345+219_345+221dup
ENST00000650005.1:c.453+219_453+221dup (HSD17B3)	ENSP00000498121.1:n.453+219_453+221dup
ENST00000650386.1:c.453+219_453+221dup (HSD17B3)	ENSP00000497464.1:n.453+219_453+221dup
ENST00000375262.3:c.453+219_453+221dup (HSD17B3)	ENSP00000364411.2:n.453+219_453+221dup
ENST00000375263.7:c.453+219_453+221dup (HSD17B3)	ENSP00000364412.3:n.453+219_453+221dup
ENST00000463517.1:n.273_275dup (HSD17B3)
NM_000197.1:c.453+219_453+221dup (HSD17B3)	NP_000188.1:n.453+219_453+221dup
XM_006717095.2:c.453+219_453+221dup (HSD17B3)	XP_006717158.1:n.453+219_453+221dup
XM_011518618.1:c.453+219_453+221dup (HSD17B3)	XP_011516920.1:n.453+219_453+221dup
XM_011518619.1:c.453+219_453+221dup (HSD17B3)	XP_011516921.1:n.453+219_453+221dup
XM_011518620.1:c.345+219_345+221dup (HSD17B3)	XP_011516922.1:n.345+219_345+221dup
XM_011518621.1:c.453+219_453+221dup (HSD17B3)	XP_011516923.1:n.453+219_453+221dup
XR_930147.1:n.1288+3866_1288+3868dup (HSD17B3-AS1)
XR_930148.1:n.1288+3866_1288+3868dup (HSD17B3-AS1)
NM_000197.2:c.453+219_453+221dup (HSD17B3) MANE Select	NP_000188.1:n.453+219_453+221dup
XM_011518618.2:c.453+219_453+221dup (HSD17B3)	XP_011516920.1:n.453+219_453+221dup
XM_011518619.2:c.453+219_453+221dup (HSD17B3)	XP_011516921.1:n.453+219_453+221dup
XM_017014671.1:c.453+219_453+221dup (HSD17B3)	XP_016870160.1:n.453+219_453+221dup
XM_017014672.1:c.453+219_453+221dup (HSD17B3)	XP_016870161.1:n.453+219_453+221dup
XM_017014673.2:c.453+219_453+221dup (HSD17B3)	XP_016870162.1:n.453+219_453+221dup
XM_017014674.1:c.345+219_345+221dup (HSD17B3)	XP_016870163.1:n.345+219_345+221dup
XM_017014675.1:c.291+219_291+221dup (HSD17B3)	XP_016870164.1:n.291+219_291+221dup
XM_017014677.1:c.-484+219_-484+221dup (HSD17B3)	XP_016870166.1:n.-484+219_-484+221dup
XM_024447529.1:c.291+219_291+221dup (HSD17B3)	XP_024303297.1:n.291+219_291+221dup
XR_002956778.1:n.2887+219_2887+221dup (HSD17B3)